Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
Y | g.12833695G>A | CA414998627 | USP9Y | c.5029G>A (p.Gly1677Ser) n.5041G>A c.4795G>A (p.Gly1599Ser) c.5044G>A (p.Gly1682Ser) | |
Y | g.12833695G>C | CA414998628 | USP9Y | c.5029G>C (p.Gly1677Arg) n.5041G>C c.4795G>C (p.Gly1599Arg) c.5044G>C (p.Gly1682Arg) | |
Y | g.12833695G>T | CA414998630 | USP9Y | c.5029G>T (p.Gly1677Cys) n.5041G>T c.4795G>T (p.Gly1599Cys) c.5044G>T (p.Gly1682Cys) | |
Y | g.12833696G>A | CA414998634 | USP9Y | c.5030G>A (p.Gly1677Asp) n.5042G>A c.4796G>A (p.Gly1599Asp) c.5045G>A (p.Gly1682Asp) | |
Y | g.12833696G>C | CA414998636 | USP9Y | c.5030G>C (p.Gly1677Ala) n.5042G>C c.4796G>C (p.Gly1599Ala) c.5045G>C (p.Gly1682Ala) | |
Y | g.12833696G>T | CA414998632 | USP9Y | c.5030G>T (p.Gly1677Val) n.5042G>T c.4796G>T (p.Gly1599Val) c.5045G>T (p.Gly1682Val) | |
Y | g.12833697T>A | CA519901450 | USP9Y | c.5031T>A (p.Gly1677=) n.5043T>A c.4797T>A (p.Gly1599=) c.5046T>A (p.Gly1682=) | |
Y | g.12833697T>C | CA519901452 | USP9Y | c.5031T>C (p.Gly1677=) n.5043T>C c.4797T>C (p.Gly1599=) c.5046T>C (p.Gly1682=) | |
Y | g.12833697T>G | CA519901453 | USP9Y | c.5031T>G (p.Gly1677=) n.5043T>G c.4797T>G (p.Gly1599=) c.5046T>G (p.Gly1682=) | |
Y | g.12833698G>A | CA414998638 | USP9Y | c.5032G>A (p.Glu1678Lys) n.5044G>A c.4798G>A (p.Glu1600Lys) c.5047G>A (p.Glu1683Lys) | |
Y | g.12833698G>C | CA414998640 | USP9Y | c.5032G>C (p.Glu1678Gln) n.5044G>C c.4798G>C (p.Glu1600Gln) c.5047G>C (p.Glu1683Gln) | |
Y | g.12833698G>T | CA414998642 | USP9Y | c.5032G>T (p.Glu1678Ter) n.5044G>T c.4798G>T (p.Glu1600Ter) c.5047G>T (p.Glu1683Ter) | |
Y | g.12833699A>C | CA414998645 | USP9Y | c.5033A>C (p.Glu1678Ala) n.5045A>C c.4799A>C (p.Glu1600Ala) c.5048A>C (p.Glu1683Ala) | |
Y | g.12833699A>G | CA414998646 | USP9Y | c.5033A>G (p.Glu1678Gly) n.5045A>G c.4799A>G (p.Glu1600Gly) c.5048A>G (p.Glu1683Gly) | |
Y | g.12833699A>T | CA414998648 | USP9Y | c.5033A>T (p.Glu1678Val) n.5045A>T c.4799A>T (p.Glu1600Val) c.5048A>T (p.Glu1683Val) | |
Y | g.12833700A>C | CA414998651 | USP9Y | c.5034A>C (p.Glu1678Asp) n.5046A>C c.4800A>C (p.Glu1600Asp) c.5049A>C (p.Glu1683Asp) | |
Y | g.12833700A>G | CA519901463 | USP9Y | c.5034A>G (p.Glu1678=) n.5046A>G c.4800A>G (p.Glu1600=) c.5049A>G (p.Glu1683=) | |
Y | g.12833700A>T | CA414998650 | USP9Y | c.5034A>T (p.Glu1678Asp) n.5046A>T c.4800A>T (p.Glu1600Asp) c.5049A>T (p.Glu1683Asp) | |
Y | g.12833701C>A | CA414998653 | USP9Y | c.5035C>A (p.Pro1679Thr) n.5047C>A c.4801C>A (p.Pro1601Thr) c.5050C>A (p.Pro1684Thr) | |
Y | g.12833701C>G | CA414998655 | USP9Y | c.5035C>G (p.Pro1679Ala) n.5047C>G c.4801C>G (p.Pro1601Ala) c.5050C>G (p.Pro1684Ala) | |
Y | g.12833701C>T | CA414998657 | USP9Y | c.5035C>T (p.Pro1679Ser) n.5047C>T c.4801C>T (p.Pro1601Ser) c.5050C>T (p.Pro1684Ser) | |
Y | g.12833702C>A | CA337720909 | USP9Y | c.5036C>A (p.Pro1679His) n.5048C>A c.4802C>A (p.Pro1601His) c.5051C>A (p.Pro1684His) | dbSNP |
Y | g.12833702C= | CA2470560445 | USP9Y | c.5036C= (p.Pro1679=) n.5048C= c.4802C= (p.Pro1601=) c.5051C= (p.Pro1684=) | |
Y | g.12833702C>G | CA414998660 | USP9Y | c.5036C>G (p.Pro1679Arg) n.5048C>G c.4802C>G (p.Pro1601Arg) c.5051C>G (p.Pro1684Arg) | |
Y | g.12833702C>T | CA414998662 | USP9Y | c.5036C>T (p.Pro1679Leu) n.5048C>T c.4802C>T (p.Pro1601Leu) c.5051C>T (p.Pro1684Leu) | |
Y | g.12833703T>A | CA519901471 | USP9Y | c.5037T>A (p.Pro1679=) n.5049T>A c.4803T>A (p.Pro1601=) c.5052T>A (p.Pro1684=) | |
Y | g.12833703T>C | CA519901474 | USP9Y | c.5037T>C (p.Pro1679=) n.5049T>C c.4803T>C (p.Pro1601=) c.5052T>C (p.Pro1684=) | |
Y | g.12833703T>G | CA519901475 | USP9Y | c.5037T>G (p.Pro1679=) n.5049T>G c.4803T>G (p.Pro1601=) c.5052T>G (p.Pro1684=) | |
Y | g.12833704G>A | CA414998665 | USP9Y | c.5038G>A (p.Val1680Ile) n.5050G>A c.4804G>A (p.Val1602Ile) c.5053G>A (p.Val1685Ile) | |
Y | g.12833704G>C | CA414998668 | USP9Y | c.5038G>C (p.Val1680Leu) n.5050G>C c.4804G>C (p.Val1602Leu) c.5053G>C (p.Val1685Leu) | |
Y | g.12833704G>T | CA414998666 | USP9Y | c.5038G>T (p.Val1680Phe) n.5050G>T c.4804G>T (p.Val1602Phe) c.5053G>T (p.Val1685Phe) | |
Y | g.12833705T>A | CA414998670 | USP9Y | c.5039T>A (p.Val1680Asp) n.5051T>A c.4805T>A (p.Val1602Asp) c.5054T>A (p.Val1685Asp) | |
Y | g.12833705T>C | CA414998671 | USP9Y | c.5039T>C (p.Val1680Ala) n.5051T>C c.4805T>C (p.Val1602Ala) c.5054T>C (p.Val1685Ala) | |
Y | g.12833705T>G | CA414998673 | USP9Y | c.5039T>G (p.Val1680Gly) n.5051T>G c.4805T>G (p.Val1602Gly) c.5054T>G (p.Val1685Gly) | |
Y | g.12833706T>A | CA519901486 | USP9Y | c.5040T>A (p.Val1680=) n.5052T>A c.4806T>A (p.Val1602=) c.5055T>A (p.Val1685=) | |
Y | g.12833706T>C | CA519901484 | USP9Y | c.5040T>C (p.Val1680=) n.5052T>C c.4806T>C (p.Val1602=) c.5055T>C (p.Val1685=) | |
Y | g.12833706T>G | CA519901482 | USP9Y | c.5040T>G (p.Val1680=) n.5052T>G c.4806T>G (p.Val1602=) c.5055T>G (p.Val1685=) | |
Y | g.12833707A>C | CA414998675 | USP9Y | c.5041A>C (p.Asn1681His) n.5053A>C c.4807A>C (p.Asn1603His) c.5056A>C (p.Asn1686His) | |
Y | g.12833707A>G | CA414998677 | USP9Y | c.5041A>G (p.Asn1681Asp) n.5053A>G c.4807A>G (p.Asn1603Asp) c.5056A>G (p.Asn1686Asp) | |
Y | g.12833707A>T | CA414998678 | USP9Y | c.5041A>T (p.Asn1681Tyr) n.5053A>T c.4807A>T (p.Asn1603Tyr) c.5056A>T (p.Asn1686Tyr) | |
Y | g.12833708A>C | CA414998681 | USP9Y | c.5042A>C (p.Asn1681Thr) n.5054A>C c.4808A>C (p.Asn1603Thr) c.5057A>C (p.Asn1686Thr) | |
Y | g.12833708A>G | CA414998682 | USP9Y | c.5042A>G (p.Asn1681Ser) n.5054A>G c.4808A>G (p.Asn1603Ser) c.5057A>G (p.Asn1686Ser) | |
Y | g.12833708A>T | CA414998684 | USP9Y | c.5042A>T (p.Asn1681Ile) n.5054A>T c.4808A>T (p.Asn1603Ile) c.5057A>T (p.Asn1686Ile) | |
Y | g.12833709T>A | CA414998686 | USP9Y | c.5043T>A (p.Asn1681Lys) n.5055T>A c.4809T>A (p.Asn1603Lys) c.5058T>A (p.Asn1686Lys) | |
Y | g.12833709T>C | CA519901494 | USP9Y | c.5043T>C (p.Asn1681=) n.5055T>C c.4809T>C (p.Asn1603=) c.5058T>C (p.Asn1686=) | |
Y | g.12833709T>G | CA414998688 | USP9Y | c.5043T>G (p.Asn1681Lys) n.5055T>G c.4809T>G (p.Asn1603Lys) c.5058T>G (p.Asn1686Lys) | |
Y | g.12833710C>A | CA414998689 | USP9Y | c.5044C>A (p.Leu1682Ile) n.5056C>A c.4810C>A (p.Leu1604Ile) c.5059C>A (p.Leu1687Ile) | |
Y | g.12833710C>G | CA414998694 | USP9Y | c.5044C>G (p.Leu1682Val) n.5056C>G c.4810C>G (p.Leu1604Val) c.5059C>G (p.Leu1687Val) | |
Y | g.12833710C>T | CA414998692 | USP9Y | c.5044C>T (p.Leu1682Phe) n.5056C>T c.4810C>T (p.Leu1604Phe) c.5059C>T (p.Leu1687Phe) | |
Y | g.12833711T>A | CA414998696 | USP9Y | c.5045T>A (p.Leu1682His) n.5057T>A c.4811T>A (p.Leu1604His) c.5060T>A (p.Leu1687His) |